Gerd Mink/Klaus Wachtel

Guide to “Genealogical Queries – Acts

(Phase 3)

Preface

This guide is based on Gerd Mink’s “Guide to ‘Genealogical Queries’ (Version 2.0)”, online here <http://intf.uni-muenster.de/cbgm2/guide_en.html>.

“Genealogical Queries – Acts (Phase 3)” is designed to be used in connection with the Editio Critica Maior (ECM) of the Acts of the Apostles (2017).

 “Genealogical Queries” provides five web-based modules that permit investigation of genealogical relationships inherent in the New Testament textual tradition.

The data brought together in the Editio Critica Maior (ECM) has been analysed and structured on the basis of the Coherence-Based Genealogical Method (CBGM).

One important feature of the CBGM is its potential to improve results through an iterative procedure. First, local stemmata of the variants are constructed taking into account pregenealogical coherence (see below). As a whole, the local stemmata comprise a first overview of genealogical relationships between the manuscript texts that attest the genealogically arranged variants. Based on this newly derived external criterion, the local stemmata are put to the test and revised.

The printed volume represents the result of the third iteration through the entire material (phase 3). The database behind phase 3, however, reflects the state of work that resulted from phase 2. So the user can review how we worked on the text and the local stemmata in phase 3, which forms the basis of the printed edition. The state of work reached at the end of phase 3, consequently, would be the basis for phase 4 which will be carried out, at the latest, when a second edition of ECM Acts is due.

Hence, what we present in “Genealogical Queries” is still a work in progress.

The software’s layout, functionality and user guidance will continue to be enhanced. Even now the program can be employed to examine the data, assess the stability of relationships, and so on. Due to continuing revision of the local stemmata, results obtained with the program today may differ from those obtained tomorrow. Nevertheless, it remains a useful analytical tool. Among many current uses, the program can be employed to examine relationships between manuscripts, highlighting various degrees of stability, thus helping to establish whether the ongoing revision process is likely to change ancestor-descendant relationships in particular cases.

 

Important: When results achieved by the CBGM are used, attention has to be paid to the data source on which they are based. This applies to “Genealogical Queries” itself as well as to literature.

 

0. Database and Premises

The ECM Acts apparatus, which work in Phase 3 was based on, has 7466 variant passages. For every instance a local stemma of variants has been created. Each stemma represents a hypothesis about which variant originates from which, thus declaring variants as prior (source variants) or posterior in their relations with one another. (In cases where a hypothesis appeared to be too unreliable, we refrained from naming a specific source variant and entered a question mark in the source field.)

The source variant is not posterior to any other variant of the same passage. It represents the starting point for the entire textual history at this place, and is thus considered to be part of the initial text of the tradition. Generally, the initial text is consistent with the base text of the ECM. There are, however, a number of instances where we have abstained from re-constructing the initial text by means of the CBGM, and such cases have been treated as if they were lacunae in the initial text. A hypothetical witness “A” was assigned to the hypothetical initial text.

The local stemmata of the variants are based on the usual text critical methods. Additionally, at the first compilation of these stemmata, the pre-genealogical coherence was examined. This type of coherence is solely based on the agreement of witnesses and is characterized by the statement:
        Witness x agrees with witness y in n out of all cases (or p % of cases).

If the pre-genealogical coherence between the attestations of two variants is very low, a genealogical relation between those two variants can be regarded as highly unlikely.

The local stemmata of the variants also establish a genealogical relation between the witnesses. This results from the fact that when two witnesses are compared across all variant passages, one is associated with a source variant more often than the other (unless the respective counts are equal). A genealogical coherence emerges, consistent with two statements:
        In n out of all cases (or p % of cases), witness x reads the source variant of the variant associated with witness y.
        In n out of all cases (or p % of cases), witness y reads the source variant of the variant of witness x.      
This results in one of the following three statements being true:
        Witness x reads the respective source variant in more cases than does witness y.
        Witness y reads more cases of the respective source variant than does witness x.
        Witness x and witness y read the respective source variant with equal frequency.

If the first of the three statements applies, witness x is a potential ancestor of witness y. If the second statement applies, then witness y is a potential ancestor of witness x. If the third statement applies, there is no genealogical direction between the two witnesses.

Important! We consider as a witness, not the manuscript itself, but the state of the text (without corrections) in a continuous text manuscript. Because the text of a manuscript can be much older than the manuscript itself, a witness that is preserved in a late manuscript (e.g. 10th century) can be a potential ancestor of a witness preserved in an early manuscript (e.g. 5th century).

The stemmatic coherence, which is the definite, simplest hypothesis about the most elementary genealogical connection between all witnesses, has not yet been implemented in the “Genealogical Queries” facility.

More...

1. “Local Stemmata” Module

This module documents the local stemmata, which are graphical representations of the presumed genealogy of variants. Local stemmata are only included for variants assigned to the first hands of Greek continuous text manuscripts.

In order to display a local stemma, a variant address that conforms to the ECM system has to be entered into the input form using numbers for chapter, verse, and beginning and ending word(s) of the variant passage.

As a rule, variant a appears at the top of the local stemma, being the text of the reconstructed initial text “A”. A question mark is placed at the top of the local stemma in passages where we abstained from a reconstruction of the initial text for the purposes of genealogical analyses (e.g. 1:6/10). A question mark was also used whenever the source of a variant could not be determined (e.g. 2:36/18-30). In such cases where we have here a particularly impressive example, “?” does not represent one common source variant. Instead, the respective source variant, to which the arrows point, is uncertain. In the present example, the source variant is uncertain in five instances. 

Note: A local stemma of variants may contain two instances of the same variant (e.g. 2:36/18-30). For example, a variant d may appear as d1 and d2. In such cases, a variant has been divided logically into two due to profound genealogical divergences. This makes it possible to relate different parts of the attestation to witnesses of different variants.

If variant a is split as in 2:40/10, the a attestation has an incoherent part. Consequently a “?” is placed in the source field for this part. In the present example, variant a is identified as initial text and as the source of variant b. A part of the a attestation, however, does not align with the rest of the witnesses supporting a but has its first potential ancestor in the b attestation, if connectivity is set to “Low” in the “Coherence in Attestation” module (see below). Several reasons are conceivable for this situation. The divergent witnesses may have, all or in part, developed variant a from b independently; some or all may have copied a from closely related but now lost witnesses of a; or they may have copied a via contamination with a lost or still extant witness of a. At any rate, the genealogy of the incoherent part of the a attestation is questionable and must not be treated like straightforward instances of a>b relationships.

 

2. “Potential Ancestors and Descendants” Module

a. Purpose of the Module

This module analyses the genealogical coherence between witnesses and can thus differentiate between potential ancestors and descendants. The relation between ancestor and descendant, and thus the genealogical coherence, is established by the proportion of variants in a witness that are prior (source variants) or posterior compared to the corresponding proportions of the compared witnesses. The degree of agreement determines the strength of the genealogical coherence.

The genealogical coherence between ancestor and descendant is determined by which witness contains more prior variants, and the strength of coherence corresponds to the level of agreement between ancestor and descendant.

The “Potential Ancestors and Descendants” module allows a sound judgment to be formed about the text-historical environment of a witness. It also permits a good guess to be made concerning which witnesses have the potential to be ancestors in a stemma.

b. The Data Entry Form

In general, Gregory-Aland manuscript numbers are used to identify witnesses in all data entry forms. Normally, only continuous text manuscripts and lectionaries are processed; however, the option to include fragmentary texts exists. The option to include fragments will normally be waived because (1) due to their small extent they are not very significant and therefore only rarely play a role in the genealogical analysis, and (2) they undermine clarity. When included, minor fragments often occupy the beginning or end of the list of results. If they cover passages that barely vary then, they tend to exhibit 100% agreement with nearly all witnesses. On the other hand, they tend towards the opposite extreme in passages where there is a lot of variation. (As an example, take witness 307 and choose the ‘Include Fragments’ option.)

In addition to the potential ancestors, the potential descendants can be displayed as well. This is of interest if one wants to see the entire close environment of a witness and especially if one assumes an unusual witness to have no more descendants.

The data source is set to “All chapters of Acts” by default, but it can be restricted to individual chapters. Choosing a single chapter may be interesting if there is reason to assume that the textual character of a witness changes so that it may have had different exemplars.

c. The Result

The header displays four percentages, referring to the witness in question, which help to put the agreement values in the table below into perspective: the share of variants pertaining to the majority text (MT and MT/P)1, the percentage of the average agreement (AA) and the median agreement (MA) with all witnesses included.

MT indicates the percentage of majority readings at passages where the respective manuscript is extant and MT is defined. MT/P indicates the share of majority readings on the basis of all variant passages where the respective manuscript is extant.2

With the default options, the result presents the potential ancestors (W2 = witness 2) of the selected witness (W1 = witness 1) sorted in descending order according to the degree of agreement with W1. (Try witness 81, for example.) Levels of agreement are found as percentages under the heading PERC1 (= percentage 1) or as absolute numbers under the heading EQ (= equal). These values are given with reference to the total number of variant passages that can be found in both W1 and W2. This total appears under the heading PASS (= passages). The highest possible number is 7466, if both compared witnesses contain all variant passages of Acts.

With all genealogical evaluations, the assumed priority or posteriority of variants plays a decisive role. Where variants are called prior or posterior in the following, these statements refer to assumptions established in the local stemmata of variants.

The column W1<W2 shows the number of cases where W2 has a variant prior to the one in W1, meaning a variant from which the variant in W1 has presumably developed. The column W1>W2 shows the number of cases where W1 contains the prior variant. A higher value in W1<W2 compared to W1>W2 characterizes W2 as potential ancestor. The difference between both values also makes a statement about the stability of the relation of W1 and W2 (the so-called “particular textual flow”). To give an example, the relation between 424 and 607 can be inverted if the genealogy of their variants is changed at only one instance.

If the values in W1<W2 and in W1>W2 are equal, there is no genealogical direction between the witnesses. In this case, a “-” appears in column D (= direction). These undirected genealogical relationships must be taken into account, especially in cases of a close relationship between W1 and W2 (cf. 607 and 642). In such instances, too, the situation would change if the genealogy of variants were assessed differently at only one passage. The result would be a directed genealogical relationship.

In column NR (= number), the potential ancestors are ranked according to their degree of agreement. If ancestors have the same degree of agreement they receive the same ranking number. If the option “Include Fragments and Undirected Relationships” has been chosen, the column NR contains a “0” if (1) an undirected genealogical relationship exists (e.g. 642 in the table referring to 607), or (2) if the number of variant passages shared by W1 and W2 does not reach a half of the passages extant in W1 (cf. 206s, 0294, 0120 for W1=607). If a genealogical direction nevertheless exists between the witnesses, a “>” will appear in column D in the second case.

At any rate, the “0” means that the pertinent witnesses under W2 are not included as potential ancestors in subsequent genealogical evaluations.

A high rank in column NR improves the odds that a potential ancestor is also a stemmatic ancestor. Since a stemma should explain the state of a text based on as small a number of contamination sources as possible, even a highly ranked (which means very similar) witness can be superfluous when constructing a stemma. This is because there may be one or more other highly ranked witnesses as contamination sources that explain all variants of the descendant without needing the one that has a higher rank. According to Ockham’s razor, a stemma that requires fewer witnesses is preferable to one with more.

In column UNCL (= unclear) one can find the number of variant passages where no decision has been made about whether W1 or W2 contains the prior variant.

Column NOREL (= no relation) displays the number of variant passages where W1 and W2 read different variants that have no direct relation to each other (e.g. if W1 reads variant b and W2 variant c, but the prior variant for both is variant a).

If the option “Show Descendants” is selected, potential descendants are also displayed. The list conforms in structure to the one for potential ancestors except in this case the values in column W1<W2 are less than those in column W1>W2.

d. How to interpret the result?

(Example witness 307, default options)

The hypothetical initial text (witness “A”) occupies the highest rank among the potential ancestors of witness 307. If “A” is near the top of such a list, witness W1 is of special interest. In such cases, W1 may reasonably be presumed to have conserved the oldest text at some instances without the intermediation of any other surviving witness. However, the level of agreement also has to be taken into account. Since nearly all textual links are missing in the oldest textual tradition, a value of more than 91% agreement with “A” is good. This value is surpassed only by 24 witnesses in relationship with “A”.

The following parameters may help to assess which agreement values can be regarded as relatively high or low. “A” agrees with the majority text (MT) at 86.33%. The average agreement (AA) of all witnesses with “A” is 89.30%. The median (MA) (above and below which the agreement values of respectively one half of the witnesses are positioned) is 89.29%. Tip: A list of all relations with “A” in descending order is displayed, if you enter “A” in this module.

 

307 agrees with the majority text (MT) at 86.28%. The average agreement (AA) of all witnesses with 307 is 86.66%. The median (MA) (above and below which the agreement values of respectively one half of the witnesses are positioned) is 87.00%.

The special quality of 307 is demonstrated already by the small number of witnesses in its list of potential ancestors. At 88.5-87.1 %, the agreements with 03, 33, 02, and 01 (all of them first-rank witnesses) are still good for older levels of the tradition. They can all be considered as sources of contamination taking into account that the intermediate witnesses, by which the connection to the earliest layers of transmission could be established, are obviously lost. Nevertheless, close relatives of 307 from later levels of the tradition survive, including many witnesses whose agreement values are clearly higher than the MT value of 307, but still do not rank among its potential ancestors.

If the option “Show Descendants” is chosen, a large number of close relatives of 307 are displayed featuring high agreement values. With these, again, the differences between the figures under W1<W2 and W1>W2 have to be considered. If the difference is minor, a potential descendant could become a potential ancestor by changing a few local stemmata.

A comparison of as many such tables as possible will make it very clear how the different values of agreement and the characteristic way these values decrease should be understood.

 (Example witness 81, Option “Show Descendants”)

The list of potential ancestors is much shorter than that of 307. It shows only two witnesses apart from “A”, 03, and P74. “A” is in first place at an excellent agreement value, exceeded only by the values of 03 and P74.

There are no particularly close relatives among the potential descendants. Only the closest one, 02, features differences between W1<W2 and W1>W2 high enough to consider a possible reversal of the genealogical relationship. If the assessment of only four passages would change in favor of the variants supported by 02, this witness would become a potential ancestor of 81.

 (Example witness 1735, Option “Show Descendants”)

1735, too, is a witness without very close relatives, as is shown by both the list of potential ancestors and descendants. 18 and 35 appear at ranks 1 and 2, “A” at rank 4. 18 and 35 represent the Kr strand of the Byzantine text. As 1735 agrees less with the majority text than with these witnesses, it shows a clear tendency towards the Kr text. The relative closeness to “A” suggests a high quality copy in terms of the scribe’s diligence.

  

3. “Comparison of Witnesses” Module

a. Purpose of the Module

This module allows comparison of the relationship of witnesses from writing to writing in order to detect any changes of Vorlagen or, rather, changes of contamination sources. If there are any conspicuous changes of the agreement values or the values under W1<W2 and W1>W2 for part of the corpus, the matter can be pursued by looking at the potential ancestors of the witnesses based on the data of single letters.

b. The Data Entry Form

The witnesses to be compared can be entered here. Principle uses of this module include comparison of a witness with the hypothetical initial text (witness “A”) and comparison of witnesses that are relatively closely related.

c. The Result

The result places the compared witnesses under W1 and W2, and the genealogical direction of the relationship under DIR (= direction). (The DIR column has “-->” if W1>W2 has a higher value than W1<W2, or “<--” for the opposite case.) Figures in a row refer to the letter given under the heading CHAP (= chapter); in the last row (CHAP = Act), values for the entire corpus are shown. Column NR contains the rank in the list of potential ancestors of the descendant witness, based on the data source indicated in the WRIT column. All other columns have the same meaning as in the “Potential Ancestors and Descendants” module.

If a chapter is missing under CHAP, at least one of the compared witnesses is lacking there. By selecting “View Differences”, the diverging variants of the compared witnesses can be displayed chapter by chapter. The table displays the compared witnesses under W1 and W2 and the respective variants under VAR1 and VAR2. The entry under DIR indicates the genealogical direction between the variants. “U” (= unclear) appears in this column if no decision was made regarding the pair of variants in question. “N” (= no relation) appears if no direct relation between the variants was established.

d. How to interpret the result?

(Example witness “A” and 81)

There is a high level of agreement for each data source, with extremely high percentages in chapters 3, 8 and 24. There are no entries for chapters 5 and 6 because 81 has a large lacuna there.

(Example witness 81 and 03)

The special quality of 81 is confirmed by the fact that it has more priority readings than 03 in several chapters.

(Example witness 18 and 35)

These two important representatives of the Byzantine text are very similar. The difference of the values under W1<W2 and W1>W2 is either very insignificant or zero. It is not significant that the genealogical direction in chapters 1, 15, 24, and 28 differs from the general trend. The differences are so slight as to indicate a weakly developed trend, if any.

 

4. “Coherence in Attestations” Module

a. Purpose of the Module

This module allows for the creation of so-called textual flow diagrams within attestations and also displays possible connections to attestations of other variants at the same variant passage.

Excursus: Textual flow is the consequence of a genealogical decline between the witnesses. The textual flow contains variants that constitute agreement or disagreement between witnesses.

We differentiate between different kinds of textual flow. The general textual flow commonly proceeds from earlier to later forms of text. The position of any witness within the general textual flow can be determined by the genealogical coherence of its closest relatives (compare the “Potential Ancestors and Descendants” Module). The particular textual flow is the one that can be established between ancestor and descendant respectively. It contains variants adopted by the descendant and those taken by the descendant as starting points of change. The global textual flow prevails within a global stemma of the witnesses and presumes stemmatic coherence, i.e. a definite hypothesis about which preferably small combination of ancestors entirely explains the text of a descendant. The local textual flow is the one taking place within a certain attestation or within the attestations of all variants at a certain text passage. The local textual flow can be based upon genealogical or stemmatic coherence.

This module looks at local textual flow based on genealogical coherencies.

b. The Data Entry Form

The variant address should be entered based on the common address system of the ECM (chapter, verse, word number of the beginning and end of the variant passage, and letter address of the variant).

Normally, the entire book of Acts should be selected as the data source. The genealogical coherencies for the relations of the witnesses that have been collected by analysis of the entire corpus will then form the base of the TFD.

If you have selected the “Book of Acts” option and find incoherencies that might suggest witnesses within the corpus have changed Vorlage, you could instead select a single chapter as the base.

It is possible to conduct an evaluation of the connectivity of a variant. Connectivity is the capacity of a variant to connect ancestors and descendants genealogically. It depends on two parameters: (1) the degree of relationship of the witnesses involved, that is on their general level of agreement, and (2) the character of the variant. In other words, for closely related witnesses even the agreement of insignificant details supports the relationship — the common variants are connective. With a lower degree of general agreement, one would rather consider multiple coincidental emergence of a variant if its character advises us to do so. In cases where coincidental multiple emergence is unlikely, the variant in question is connective, even for witnesses that have a lesser degree of relationship.

Depending on the assessment of connectivity, the potential ancestors are analyzed as long as the appropriate ranking number is not exceeded. The default setting is “Lower”. This option is recommendable for Acts because, in comparison with the Catholic Letters, there is less conspicuous variation in general. The option “Higher” can be selected, if the variant appears more connective than usual. Moreover, a user-defined value may be entered. The option “Absolute” enforces coherence of all witnesses of the same variant. This option offers a good way to see how remote the witnesses of an attestation are, since the ranking number from the list of potential ancestors is displayed (see below).

It is possible to select the variant that constitutes the initial text of the tradition (“Initial Reading”, IR). In the default setting, the program assumes that this is variant a, regardless of whether or not a decision about the initial text was made in the local stemma. The user can set any variant of a passage as initial or leave the decision open by entering “?”.

c. The Result

The result is a graph displaying the local textual flow based on genealogical coherencies. The arrows point respectively from the (potential) ancestor to the (potential) descendant within the attestation. If one looked up a list of potential ancestors for a descendant in the graph shown here in the module “Potential Ancestors and Descendants”, one would find a ranking number in column NR for the ancestor from which the descendant in this graph is derived. If this ranking number is 1, it will not be noted for the descendant in the graph since this case dominates. If the ranking number is greater than 1, it will be displayed together with the descendant after a slash. The level of connectivity selected in the data entry form determines up to which ranking number the potential ancestors will be charted on the graph.

If no potential ancestor can be found for a descendant within the same attestation, then the attestations of other variants at this place will be searched. In each case, together with the corresponding potential ancestor, the locations (variants) will be displayed outside the frame that encircles the current attestation. Next, the ranking number the potential ancestor obtains in the ancestor list of the descendant will be displayed along with the identification of the ancestor.

Thus, one can obtain an overview as to whether or not a variant can be deduced from the current variant.

The contents of the graph can also be displayed as a table (“Show Table”). This is useful if the course of the arrows is too confusing. In the chart, the witnesses will be arranged in generations (G1-G16). G0 is the generation of witnesses located with the variant from which the current one is deducible. The identification of this variant is to be found under VARID. N0-N15 contain the ranking numbers. The reading of such a chart will be explained in the next example.

There is also a “Show Local Stemma” option that can be used to display a local stemma of the variants at the selected passage. Such local variant stemmata have been created for all variant passages in order to calculate the genealogical coherence of the witnesses in a writing or in the entire corpus based on the variant relations. In the module “Coherence in Attestations”, those genealogical coherencies of witnesses are projected back to the variants of a variant passage. In doing so, it may happen that relations presumed in the local stemma of the variants are not compatible with the result obtained in this module (e.g. if the local stemma deduces one variant from another one for which there is no relation through genealogically coherent witnesses according to the result of this module). Inconsistencies like this one are important indications that the local stemma should probably be revised. The local stemmata are based on genealogical data as collected for the single writings. Note that variant identifiers can be split (e.g. b into b1 and b2). Cf. the explanations on the module “Local Stemmata”.

d. How to interpret the result?

Example 11:8/12-18c, default options

The entire attestation of the variant is visible in the frame, divided into two branches. In view of the selected connectivity, this result indicates that the variant may have evolved twice. With Connectivity set to 10 (Con=10), the textual flow diagram (TFD) indicates that the potential ancestors of 876 and 1739 up to rank number 10 support another variants than c. The sources are displayed outside the frame, 18 supporting f for 876, “A” for 1739. (As the first potential ancestor of 876, 424, has a lacuna here, the ancestor with rank number 2, 18/2, is displayed.)

In the chart connected to the graph (“Show Table”), you find the witnesses displayed outside the frame (from which witnesses inside the frame are derived) under G0. The variant they read is indicated under VARID. The descendants of witnesses under the heading G0 are listed under G1, e.g. 876 as descendant of 18. 18 has the ranking number 2 as potential ancestor, apparent under N0. In column G2, a descendant of 876 is found in the line of 876. Under the heading N1, one can find the ranking number that the ancestor (under G1) possesses in the ancestor list of a descendant (under G2). All these details can also be obtained with the graph.

There is still important additional information in the table. It is found in the columns PEV0, PEV1 etc (PEV = percentage of equal variants). For example, the percentage in the first line of the column PEV0, 92.695 specifies the agreement of 18 (G0) and 876 (G1). It is the same percentage we find when we look for the potential ancestors of 876 in the “Potential Ancestors” module (column PERC1). If there are several descendants of the same ancestor, they are displayed in the subsequent generation column beginning with the line in which the ancestor is listed (e.g. 429, 630 and 1751 for 2200; 522, 636, and 1490 for 429). The percentages under PEV4 show how different various agreement values can be, although the ranking number remains the same. Thus, the ranking numbers may indicate that there is a chance that a potential ancestor may become a stemmatic ancestor in an optimal substemma. The percentages of agreement, however, must additionally be consulted in order to assess the possibility of merely coincidental agreements.

At any rate, the TFD for 11:8/12-18c suggests that variant c emerged from variant f in 876, and from variant a in 1739. To put the split of the attestation to the test, set Connectivity to “Absolute” and notice the TFD produced. Now, 876 is forced into the strand led by 1739 with 1490 as potential ancestor with rank number 42. The values shown in the table behind the graph indicate an agreement rate of 89.085. To assess this value, one has to consult the list of potential ancestors of 876. It shows that the percentage of agreement of 876 with 1490 is lower than that with the majority text, but still higher than its average and median agreement rates. The agreement values descending continuously from 93.248 in 424 and 92.695 in 18, however, show how slight the chance is that 878 actually copied variant c from one of the other witnesses in the c attestation.

Example 9:3/20-22c

This variant is attested by the majority of Greek witnesses and could theoretically be the initial one according to internal criteria (see the discussion of the passage in K. Wachtel, “Constructing Local Stemmata for the ECM of Acts: Examples,” TC 20 (2015), p.10). The TFD, however, provides decisive arguments against this presumption.

If we set Initial Reading to c and Connectivity to 10, we get a coherent TFD with seven “A”-related witnesses at the top. The data behind the graph, however, show that most of the direct relationships with “A” are weak. 08 and 044 both agree with “A” at less than 90% and their lists of potential ancestors are extensive. This means that they have many special readings and are in a text with an early basic stratum. For 33, 623, and 1409, the agreement with “A” is higher. In this attestation these witnesses are featuring the best relationships with the early phases of transmission represented by “A”. For 35 and 431, the figures after the slash indicate that they have more closely related potential ancestors in other attestations. This weakens the support of the Byzantine mainstream, which is led by 35. In conclusion, this attestation is far weaker than the one for a, where all other “A”-related witnesses are assembled. Thus it is more likely that the connection with καί is secondary, probably because this appeared apt to start the report about a sudden incident. Moreover, such a change could very well occur attractive to more than one editor or scribe, which justifies setting the connectivity lower. The user may experiment with the parameters and see, for example, how the TFD is influenced by IR = a and Connectivity = Low. The graph now shows four strands with relationships to potential ancestors supporting a in the b attestation. This remains the same if you leave open the question of which variant is initial (Initial Reading = ?), although in that case, P74 takes the place of “A” as first potential ancestor of 33.

A cross check can be made by looking at the TFD for a using the same parameters (IR = ? and Connectivity = Low). The resulting graph basically shows a very coherent attestation comprising the earliest witnesses otherwise related to “A”. Only one incoherency gives reason to assume that occasionally a connection with καί was preferred to a postponed τέ.

 

5. “Coherence at Variant Passages” Module

a. Purpose of the Module

This module should assist the user to develop an overview of all the relations between the variants of a variant passage.

The result can be regarded as a summary of all results that one would receive if the module “Coherence in Attestations” was applied to all variants of a variant passage.

b. The Data Entry Form

This form is derived from the one used in the “Coherence in Attestations” module, where most of the same options are selectable (see above). Additionally, we find the option group “Display Mode”.

The “Qualified: All Interrelations” option displays relations that are possible based on the respective strongest genealogical coherence between witnesses of different variants. The “Qualified: Interrelations of the first order only” option causes a limitation of the result: relations between variants will only be displayed if — in reference to the descendant — the potential ancestor in an ancestor list has ranking number 1.

c. Result and Interpretation

Example 9:3/20-22, default option

The textual flows that emanate from potential ancestors with ranking number 1 are displayed in blue, the others in green. The numbers shown with the green relations indicate the ranking number of the potential ancestor.

For the suggested example, there is only one green arrow pointing from 429 to 323. The relationships between witnesses of a and c reflect what was said above about 9:3/20-22c as an example for applying the “Coherence in Attestations” module. In addition, the graph suggests that variants b and d are derived from c.



1 The variants of the majority text were determined by a selection of nearly pure representatives of the Byzantine text (cf. ECM III.2 Supplementary Material, 2.2 Codices Byzantini). Where these representatives point to a split Byzantine attestation, it is not possible to determine the majority reading with certainty. Such passages were not included for determining the MT value in the “Potential Ancestors and Descendants” module.

2 If x is the number of passages where the manuscript is extant, y the number of passages where the majority text is defined, z the number of passages where the manuscript agrees with the majority text, then MT = z/y and MT/P = z/x.